A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047077



Internal ID19136296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125985970..126001206hg38UCSC Ensembl
Innerchr9:128748249..128763485hg19UCSC Ensembl
Innerchr9:127788070..127803306hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3815237
hg1915237
hg1815237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695233
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047077
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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